Clinical Trial

Effect of Delivery Time on Umbilical Cord Blood Gas Parameters in Cesarean Sections Under General and Spinal Anesthesia

Study acronym: DELTA-CS
Completed
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Summary
The goal of this observational study is to evaluate the effect of neonatal delivery time on umbilical cord blood gas parameters in pregnant women undergoing elective cesarean section under general or spinal anesthesia. The study population consists of adult pregnant women aged 18-40 years with singleton term pregnancies scheduled for elective cesarean delivery. The main questions it aims to answer are: Is neonatal delivery time associated with changes in umbilical artery pH values under general and spinal anesthesia? Is neonatal delivery time associated with changes in umbilical artery base excess under general and spinal anesthesia? Researchers will compare cesarean sections performed under general anesthesia with those performed under spinal anesthesia to determine whether the relationship between delivery time and umbilical cord blood gas parameters differs between anesthesia techniques. Participants will: Undergo elective cesarean delivery under general or spinal anesthesia as part of routine clinical care Have neonatal delivery time recorded intraoperatively Have umbilical artery blood gas parameters (pH and base excess) measured immediately after birth as part of standard neonatal assessment
Protocol Amendment History 1 change
critical Trial completed 2026-05-19
Trial Details
NCT Number NCT07321041
Lead Sponsor Sisli Hamidiye Etfal Training and Research Hospital
Conditions Umbilical Cord Blood, Cesarean Section Surgery, General Anesthesia, Spinal Anesthesia, Blood Gas Analysis
Enrollment 100 participants
Start Date 2026-01-15
Primary Completion 2026-04-24 (estimated)
Study Completion 2026-04-24 (estimated)
Updated on ClinicalTrials.gov 2026-05-18